Results
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1.
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Fine mapping and identification of serum urate loci in American Indians: The Strong Heart Family Study. MedStar authors:
Year: 2019
Citation: - Scientific Reports. 9(1):17899, 2019 11 29.
Institution: - MedStar Health Research Institute
Medline publication type:
All authors: - Balakrishnan P, Best LG, Bharadwaj D, Bizon C, Canizales-Quinteros S, Chittoor G, Cole SA, Franceschini N, Haack K, Laston S, MacCluer JW, Macias-Kauffer L, Navas-Acien A, North KE, Prasad G, Umans JG, Villarreal-Molina T, Voruganti VS
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2.
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Genome-Wide Analysis of Left Ventricular Image-Derived Phenotypes Identifies Fourteen Loci Associated With Cardiac Morphogenesis and Heart Failure Development. MedStar authors:
Year: 2019
Citation: - Circulation. 140(16):1318-1330, 2019 10 15.
Institution: - MedStar Health Research Institute
Medline publication type:
All authors: - Aung N, Barnes MR, Bluemke DA, Cabrera CP, Fung K, Lima JAC, Manichaikul AW, Munroe PB, Neubauer S, Petersen SE, Piechnik SK, Rotter JI, Taylor KD, Tzanis E, Vargas JD, Warren HR, Yang C
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3.
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Replication of the effect of SLC2A9 genetic variation on serum uric acid levels in American Indians. MedStar authors:
Year: 2014
Citation: - European Journal of Human Genetics. 22(7):938-43, 2014 Jul.
Institution: - MedStar Health Research Institute
Medline publication type:
- Clinical Trial
- Journal Article
- Multicenter Study
- Research Support, American Recovery and Reinvestment Act
- Research Support, N.I.H., Extramural
All authors: - Cole SA, Comuzzie AG, Franceschini N, Haack K, Laston S, MacCluer JW, North KE, Umans JG, Voruganti VS
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4.
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Common genetic variation in the 3'-BCL11B gene desert is associated with carotid-femoral pulse wave velocity and excess cardiovascular disease risk: the AortaGen Consortium. MedStar authors:
Citation: - Circulation. Cardiovascular Genetics. 5(1):81-90, 2012 Feb 1.
Institution: - MedStar Heart & Vascular Institute
Medline publication type:
- Journal Article
- Meta-Analysis
- Research Support, N.I.H., Extramural
- Research Support, N.I.H., Intramural
- Research Support, Non-U.S. Gov't
All authors: - Abecasis GR, Andrews JS, Arfan Ikram M, Aspelund T, Bekaert S, Benjamin EJ, Cockcroft JR, De Backer GG, De Bacquer D, De Buyzere ML, De Meyer T, Dehghan A, Ding J, Eiriksdottir G, Elliott P, Erdmann J, Felix JF, Ferrucci L, Fuchsberger C, Gibson Q, Gillebert TC, Gudnason V, Hamburg NM, Harris TB, Herrington DM, Hofman A, Howard TD, Isaacs A, Jewell ES, Johnson AD, Lakatta EG, Larson MG, Launer LJ, Levy D, Liu Y, Mattace-Raso FU, McArdle PF, McEniery CM, Mitchell GF, Najjar SS, Newhouse SJ, Newman AB, O'Shaughnessy KM, Olden M, Oostra BA, Parsa A, Post WS, Psaty BM, Rietzschel ER, Rivadeneira F, Sanna S, Schut AF, Scuteri A, Segers P, Shuldiner AR, Sie MP, Sigurdsson S, Sijbrands EJ, Smith AV, Smith NL, Sutton-Tyrrell K, Tanaka T, Tarasov KV, Uda M, Uitterlinden AG, Van Bortel L, van Duijn CM, van Rijn MJ, Vasan RS, Verwoert GC, Vita JA, Wain LV, Wilkinson IB, Witteman JC, Yasmin
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5.
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Heritability estimates identify a substantial genetic contribution to risk and outcome of intracerebral hemorrhage. MedStar authors:
Citation: - Stroke. 44(6):1578-83, 2013 Jun.
Institution: - MedStar Heart & Vascular Institute
Medline publication type:
- Journal Article
- Research Support, N.I.H., Extramural
- Research Support, Non-U.S. Gov't
All authors: - Anderson CD, Ayres AM, Biffi A, Brown DL, Cuadrado-Godia E, Delgado P, Devan WJ, Falcone GJ, Fernandez-Cadenas I, Freudenberger P, Giralt-Steinhauer E, Goldstein JN, Greenberg SM, Hansen BM, International Stroke Genetics Consortium, Jagiella JM, Jimenez-Conde J, Kassis SB, Kidwell CS, Lindgren A, Meschia JF, Montaner J, Norrving B, Pera J, Roquer J, Rosand J, Rost NS, Schmidt H, Schmidt R, Schwab K, Selim M, Silliman SL, Slowik A, Soriano C, Stogerer EM, Tirschwell DL, Urbanik A, Valant V, Viswanathan A, Woo D, Worrall BB
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